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Comparison of acidity and chemical composition of summertime cloud water and aerosol at an alpine site in Northwest China: Implications for the neutral property of clouds in the free troposphere

  • Minxia Shen
  • , Jianjun Li
  • , Yali Liu
  • , Wenting Dai
  • , Gehui Wang
  • , Weining Qi
  • , Yukun Chen
  • , Xiao Guo
  • , Yifan Zhang
  • , Lu Li
  • , Yue Cao
  • , Qiao Feng
  • , Hui Su
  • , Junji Cao
  • CAS - Institute of Earth Environment
  • Guanzhong Plain Ecological Environment Change and Comprehensive Treatment National Observation and Research Station
  • Xi'an Institute for Innovative Earth Environment Research
  • East China Normal University
  • Xi'an Jiaotong University

科研成果: 期刊稿件文章同行评审

1 引用 (Scopus)

摘要

Aerosol and cloud acidity are essential to human health, ecosystem health and productivity, as well as climate effects. The main chemical composition of cloud water greatly varies in different regions, resulting in substantial differences in the pH of cloud water. However, the influences of the anthropogenic emissions of acidic gases and substances, alkaline dust components, and dicarboxylic acids (diacids) on the ground concerning the acidity of cloud water in the free troposphere of the Guanzhong Plain, China, remain clear. In this study, cloud water and PM2.5 samples were simultaneously collected in the troposphere (Mt. Hua, 2060 m a.s.l). The results indicated that the cloud water was alkaline (pH = 7.6) and PM2.5 was acidic (pH = 3.2). These results showed the neutral property of clouds collected in the heavily polluted Guanzhong Plain, although most previous studies always considered acidity as a marker of pollution. The sulfate (SO4 2−), nitrate (NO3 ), and ammonium (NH4 +) (SNA) of particulate matter and cloud water in the same period were compared. SO4 2− was dominant in particulate matters (accounting for 63.4 % of the total SNA) but substantially decreased in cloud water (only 30.1 % of the total SNA), whereas NO3 and NH4 + increased from 28.5 % and 8.2 % to 39.8 % and 30.2 %, respectively. This could be attributed to the complex formation mechanism and sources of SO4 2− and NO3 in the cloud. The results of ion balance indicated that a significant deficit of inorganic anion equivalents was observed in the cloud water samples. The high concentration of diacids in the cloud phase (1237.4 μg L−1) may facilitate the formation of salt complexes with NH4 +, thus influencing the acidity of the cloud water. The pH of cloud water has increased in recent decades due to the sustained reduction of sulfur dioxide, which may also affect the acidity of future precipitation.

源语言英语
文章编号171775
期刊Science of the Total Environment
925
DOI
出版状态已出版 - 15 5月 2024

联合国可持续发展目标

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  1. 可持续发展目标 3 - 良好健康与福祉
    可持续发展目标 3 良好健康与福祉
  2. 可持续发展目标 13 - 气候行动
    可持续发展目标 13 气候行动

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